돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 392486생성일: 2026년 10월 24일

Methylhydrazine → 2,5-dimethoxythiobenzoic acid N-methylhydrazide

https://huagongshe.com/ko/reaction/392486

반응식

참여 물질

역할이름HCID투입량
반응물MethylhydrazineHCID 6061—
반응물DicyclohexylcarbodiimideHCID 10868—
반응물2,5-Dimethoxybenzoic acidHCID 76027—
반응물Lawesson's reagentHCID 87949—
촉매4-(Dimethylamino)pyridineHCID 14284—
용매DichloromethaneHCID 6344—
용매Ethyl AcetateHCID 8857—
생성물2,5-dimethoxythiobenzoic acid N-methylhydrazideHCID 11333617116.8%

반응 단계

DCC (4.5 g, 21.8 mmol) was added in one portion to a solution of 2,5-dimethoxybenzoic acid (3.6 g, 20 mol), methylhydrazine (1.2 ml, 23 mmol) and DMAP (30 mg, cat.) in CH2Cl2 (60 ml) cooled in an ice bath. The reaction mixture was stirred overnight at room temperature. The slurry was cooled at −20° C. for 1 h and filtered. The CH2Cl2 solution was evaporated and the residue was dried in vacuum. The resulting crude product was dissolved in toluene (50 ml). To this solution was added Lawesson's reagent (5.8 g, 14 mmol). The mixture was refluxed for 40 min, cooled to room temperature, and directly subjected to silica gel column chromatography (eluent: 25% to 35% ethyl acetate in hexanes) to give the 2,5-dimethoxythiobenzoic acid N-methylhydrazide (3.7 g, yield: 82%) as off-white solid. 1H NMR (300 MHz, CDCl3): δ 6.88-6.80(m, 3H), 5.46 (s, 2H), 3.84(s, 3H), 3.82 (s, 3H), 3.28(s, 3H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06800660B2
출처 데이터셋uspto-grants-2004_10
ORD IDord-dccdbabcbe5645f88a268f092bddaa97
출처 메모uspto-grants-2004_10